Both tissue repair and regeneration are a priority in regenerative medicine. Retinitis pigmentosa (RP), a complex retinal disease characterized by the progressive loss of impaired photoreceptors, is currently lacking effective therapies: this represents one of the greatest challenges in the field of ophthalmological research. Although this inherited retinal dystrophy is still an incurable genetic disease, the oxidative damage is an important pathogenetic element that may represent a viable target of therapy. In this review, we summarize the current neuroscientific evidence regarding the effectiveness of cell therapies in RP, especially those based on mesenchymal cells, and we focus on their therapeutic action: limitation of both oxid...
Retinitis pigmentosa (RP) is one of the most common clinical subtypes of retinal degeneration (RD), ...
Unfortunately, at present, degenerative retinal diseases such as retinitis pigmentosa remains untrea...
Retinitis pigmentosa (RP) is a heterogeneous group of hereditary diseases characterized by progressi...
Unfortunately, at present, degenerative retinal diseases such as retinitis pigmentosa remains untrea...
AbstractRetinitis pigmentosa (RP) is the leading cause of hereditary blindness, and there is current...
Abstract Syndromic retinitis pigmentosa (RP) is the result of several mutations expressed in rod ph...
Syndromic retinitis pigmentosa (RP) is the result of several mutations expressed in rod photorecepto...
Retinitis pigmentosa (RP) involves a group of hereditary diseases that cause progressive and severe ...
Retinitis pigmentosa (RP) is an inherited form of retinal degeneration characterized by primary rod ...
Retinitis pigmentosa (RP) is a group of inherited retinal disorders characterized by progressive los...
Retinal degenerations are the major cause of incurable blindness characterized by loss of retinal ph...
Retinal photoreceptors are highly specialized and performing neurons. Their cellular architecture is...
Retinitis pigmentosa (RP) is an inherited retinal dystrophy characterized by progressive degeneratio...
Inherited retinal dystrophies (IRDs) are a large group of genetically and clinically heteroge-neous ...
Tvrm4 mice, a model of autosomal dominant retinitis pigmentosa (RP), carry a mutation of Rhodopsin g...
Retinitis pigmentosa (RP) is one of the most common clinical subtypes of retinal degeneration (RD), ...
Unfortunately, at present, degenerative retinal diseases such as retinitis pigmentosa remains untrea...
Retinitis pigmentosa (RP) is a heterogeneous group of hereditary diseases characterized by progressi...
Unfortunately, at present, degenerative retinal diseases such as retinitis pigmentosa remains untrea...
AbstractRetinitis pigmentosa (RP) is the leading cause of hereditary blindness, and there is current...
Abstract Syndromic retinitis pigmentosa (RP) is the result of several mutations expressed in rod ph...
Syndromic retinitis pigmentosa (RP) is the result of several mutations expressed in rod photorecepto...
Retinitis pigmentosa (RP) involves a group of hereditary diseases that cause progressive and severe ...
Retinitis pigmentosa (RP) is an inherited form of retinal degeneration characterized by primary rod ...
Retinitis pigmentosa (RP) is a group of inherited retinal disorders characterized by progressive los...
Retinal degenerations are the major cause of incurable blindness characterized by loss of retinal ph...
Retinal photoreceptors are highly specialized and performing neurons. Their cellular architecture is...
Retinitis pigmentosa (RP) is an inherited retinal dystrophy characterized by progressive degeneratio...
Inherited retinal dystrophies (IRDs) are a large group of genetically and clinically heteroge-neous ...
Tvrm4 mice, a model of autosomal dominant retinitis pigmentosa (RP), carry a mutation of Rhodopsin g...
Retinitis pigmentosa (RP) is one of the most common clinical subtypes of retinal degeneration (RD), ...
Unfortunately, at present, degenerative retinal diseases such as retinitis pigmentosa remains untrea...
Retinitis pigmentosa (RP) is a heterogeneous group of hereditary diseases characterized by progressi...